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Schizosaccharomyces pombe Rtf2 mediates site-specific replication termination by inhibiting replication restart.


ABSTRACT: Here, we identify a phylogenetically conserved Schizosaccharomyces pombe factor, named Rtf2, as a key requirement for efficient replication termination at the site-specific replication barrier RTS1. We show that Rtf2, a proliferating cell nuclear antigen-interacting protein, promotes termination at RTS1 by preventing replication restart; in the absence of Rtf2, we observe the establishment of "slow-moving" Srs2-dependent replication forks. Analysis of the pmt3 (SUMO) and rtf2 mutants establishes that pmt3 causes a reduction in RTS1 barrier activity, that rtf2 and pmt3 are nonadditive, and that pmt3 (SUMO) partly suppresses the rtf2-dependent replication restart. Our results are consistent with a model in which Rtf2 stabilizes the replication fork stalled at RTS1 until completion of DNA synthesis by a converging replication fork initiated at a flanking origin.

SUBMITTER: Inagawa T 

PROVIDER: S-EPMC2683088 | biostudies-literature | 2009 May

REPOSITORIES: biostudies-literature

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Schizosaccharomyces pombe Rtf2 mediates site-specific replication termination by inhibiting replication restart.

Inagawa Takabumi T   Yamada-Inagawa Tomoko T   Eydmann Trevor T   Mian I Saira IS   Wang Teresa S TS   Dalgaard Jacob Z JZ  

Proceedings of the National Academy of Sciences of the United States of America 20090423 19


Here, we identify a phylogenetically conserved Schizosaccharomyces pombe factor, named Rtf2, as a key requirement for efficient replication termination at the site-specific replication barrier RTS1. We show that Rtf2, a proliferating cell nuclear antigen-interacting protein, promotes termination at RTS1 by preventing replication restart; in the absence of Rtf2, we observe the establishment of "slow-moving" Srs2-dependent replication forks. Analysis of the pmt3 (SUMO) and rtf2 mutants establishes  ...[more]

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